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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 880031생성일: 2026년 10월 25일

Diisopropylcarbodiimide → Tert-butyl 4-(3-(3,4-dichlorophenyl)-1,2,4-oxadiazol-5-yl)butylcarbamate

https://huagongshe.com/reaction/880031

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylcarbodiimideHCID 12734—
반응물5-(((Tert-butoxy)carbonyl)amino)pentanoic acidHCID 545848—
반응물3,4-Dichloro-N'-hydroxybenzene-1-carboximidamideHCID 11264185—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매PyridineHCID 1049—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 4-(3-(3,4-dichlorophenyl)-1,2,4-oxadiazol-5-yl)butylcarbamateHCID 8673008430.5%

반응 단계

The 5-(tert-butoxycarbonylamino)pentanoic acid (424 mg, 1.95 mmol) was introduced into a microwave vial charged with DMAP (238 mg, 1.95 mmol) and Intermediate 20A (400 mg, 1.95 mmol). The reactants were dissolved in DMF (5 mL) and the DIC (0.304 mL, 1.95 mmol) was added. The reaction mixture was stirred at rt overnight. The reaction mixture was diluted with 3 mL of pyridine. The vial was capped and the reaction was heated in the microwave at 145° C. for 20 min. The reaction mixture was allowed to cool to rt. The reaction mixture was diluted with EtOAc and washed with water and brine. The organic portion was concentrated under reduced pressure and purified by silica gel chromatography with EtOAc/Hexane to give Intermediate 20B as a white solid (230 mg, 0.595 mmol, 30.5% yield). HPLC/MS (Method D) RT=2.40 min [M+H]+ 385.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08993557B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-18d104a6a6314c1e8f010e3ebec57d20
출처 메모uspto-grants-2015_03